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ChemicalBook--->CAS DataBase List--->638-95-9

638-95-9

638-95-9 Structure

638-95-9 Structure
IdentificationMore
[Name]

alpha-Amyrin
[CAS]

638-95-9
[Synonyms]

12-URSEN-3-BETA-OL
(3BETA)-URS-12-EN-3-OL
A-AMYRIN
ALPHA-AMYRIN
AMYRIN, A-
DELTA-AMYRIN
URS-12-EN-3-BETA-OL
VIMINALOL
alpha-Amyrenol
alpha-Amyrine
Urs-12-en-3-ol
Urs-12-en-3-ol, (3beta)-
alpha-AMYRIN hplc
A-AMYRIN WITH HPLC
Urs-12-en-3β-ol, Viminalol
(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-Octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol
3b-Hydroxyurs-12-ene
Urs-12-en-3-ol, (3b)-
[EINECS(EC#)]

211-352-1
[Molecular Formula]

C30H50O
[MDL Number]

MFCD00016754
[Molecular Weight]

426.72
[MOL File]

638-95-9.mol
Chemical PropertiesBack Directory
[Melting point ]

178-183°C
[alpha ]

D17 +91.6° (c = 1.3 in benzene)
[Boiling point ]

bp0.7 243°
[density ]

0.9600 (rough estimate)
[refractive index ]

1.4910 (estimate)
[solubility ]

DMSO (Slightly), Methanol (Slightly, Sonicated)
[form ]

neat
[pka]

15.18±0.70(Predicted)
[color ]

White to off-white
[optical activity]

+93.3 (c 5.55, C6H6)
[BRN ]

1916550
[LogP]

10.636 (est)
[CAS DataBase Reference]

638-95-9(CAS DataBase Reference)
[NIST Chemistry Reference]

«ALPHA»-amyrin(638-95-9)
[EPA Substance Registry System]

Urs-12-en-3-ol, (3.beta.)- (638-95-9)
Safety DataBack Directory
[Hazard Codes ]

Xi
[WGK Germany ]

3
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Viminalol(638-95-9).msds
Hazard InformationBack Directory
[Uses]

a-Amyrin is a natural chemical compound of the triterpene class. It is a pentacyclic triterpenol widely distributed in nature and has been isolated from a variety of plant sources such as epicuticular wax.
[Definition]

ChEBI: A pentacyclic triterpenoid that is ursane which contains a double bond between positions 12 and 13 and in which the hydrogen at the 3beta position is substituted by a hydroxy group.
[Biological Activity]

Triterpene th at has broad-spectrum analgesic properties for which the underlying mechanism is poorly understood but which may involve the inhibition of protein kinase A (PKA).
[Purification Methods]

Purify it by acetylation to the acetate followed by hydrolysis and recrystallisation from aqueous MeOH or from EtOH. The acetate when crystallised from pet ether, n-heptane or CHC
Spectrum DetailBack Directory
[Spectrum Detail]

alpha-Amyrin(638-95-9)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

638-95-9(sigmaaldrich)
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